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bioRxiv · 10.1101/786301

The Association between SLC25A15 Gene Polymorphisms and Hyperornithinemia-hyperammonemia-homocitrullinuria Syndrome: Using In Silico Analysis

Mahmoud, N. A.·Ahmed, D. T.·Mohammed, Z. O.·Altyeb, F. A.·Mustafa, M. I.·Hassan, M. A.
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Abstract

BackgroundHyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome is an autosomal recessive inborn error of the urea cycle. It is caused by mutations in the SLC25A15 gene that codes the mitochondrial ornithine transporter. The aim of this study is to detect and identify the pathogenic SNPs in SLC25A15 gene through a combination set of bioinformatics tools and their effect on the structure and function of the protein.\n\nMethodsThe deleterious SNPs in SLC25A15 are detected by various bioinformatics tools, with addition to identifying their effects on the structure and function of this gene.\n\nResults20 deleterious SNPs out 287of were found to have their own damaging effects on the structure and function of the SLC25A15 gene.\n\nConclusionThis study is the first in silico analysis of SLC25A15 using a selection of bioinformatics tools to detect functional and structural effects of deleterious SNPs. Finding the pathogenic SNPs is a promising start to innovate new, useful SNP diagnostic markers for medical testing and for safer novel therapies specifically targeting mutant SLC25A15.

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Mahmoud, N. A., Ahmed, D. T., Mohammed, Z. O., Altyeb, F. A., Mustafa, M. I., Hassan, M. A.. 2019-09-30. The Association between SLC25A15 Gene Polymorphisms and Hyperornithinemia-hyperammonemia-homocitrullinuria Syndrome: Using In Silico Analysis. https://doi.org/10.1101/786301

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